Global Regulatory Affairs Specialist (14-Mo)

Fisher Paykel Healthcare; Howick; On-site; NZD 90,000 - 120,000; Full time

Job summary

Fisher & Paykel Healthcare is seeking a Regulatory Affairs Associate/Specialist for a 14-month fixed-term role. You will support global regulatory clearance and market access for medical devices, partnering with teams to drive efficient processes and faster approvals.

The role sits at Associate or Specialist level based on candidate skills, requiring a tertiary qualification in engineering/science/law and 3+ years in a regulated industry.

Qualifications

• Tertiary qualification in engineering, science or law.
• Solutions-focused attitude with a continuous improvement mindset.
• Methodical, analytical and strategic approach with strong attention to detail.
• Strong relationship-building skills capable of engaging and influencing stakeholders.
• 3+ years of experience in a regulated industry (medical devices, pharma, food, aviation).

Responsibilities

• Lead regulatory projects and set strategy for global market access.
• Identify opportunities to improve regulatory processes and drive efficiency.
• Collaborate with cross-functional teams across the business and external stakeholders.

Skills

Planning skills

Presentation skills

Analytical thinking

Relationship building

Strategic thinking

Attention to detail

Stakeholder influence

Education

Tertiary qualification (engineering/science or law)

Job description

Fisher & Paykel Healthcare is seeking a Regulatory Affairs Associate/Specialist for a 14-month fixed-term role. You will support global regulatory clearance and market access for medical devices, partnering with teams to drive efficient processes and faster approvals.

The role sits at Associate or Specialist level based on candidate skills, requiring a tertiary qualification in engineering/science/law and 3+ years in a regulated industry.